NDC 53489-387 – Minoxidil

Minoxidil 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC53489-387

Product details

Brand name
Minoxidil
Generic name
minoxidil
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA072709
Marketed since
December 14, 1995
Listing expires
December 31, 2027
Pharmacologic class
Arteriolar Vasodilator

Active ingredients

Uses, dosage, side effects and warnings for Minoxidil →

Package NDC codes (4)

Package NDCDescriptionSince
53489-387-01100 TABLET in 1 BOTTLE (53489-387-01)Dec 14, 1995
53489-387-03250 TABLET in 1 BOTTLE (53489-387-03)Dec 14, 1995
53489-387-05500 TABLET in 1 BOTTLE (53489-387-05)Dec 14, 1995
53489-387-101000 TABLET in 1 BOTTLE (53489-387-10)Dec 14, 1995

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